학술논문

Acute responses to opioidergic blockade as a biomarker of hedonic eating among obese women enrolled in a mindfulness-based weight loss intervention trial
Document Type
article
Source
Subject
Biological Psychology
Biomedical and Clinical Sciences
Psychology
Neurosciences
Clinical Trials and Supportive Activities
Obesity
Eating Disorders
Clinical Research
Drug Abuse (NIDA only)
Nutrition
Behavioral and Social Science
Prevention
Substance Misuse
Complementary and Integrative Health
Brain Disorders
Mental Health
Good Health and Well Being
Adult
Behavior
Addictive
Binge-Eating Disorder
Body Mass Index
Body Weight
Bulimia
Eating
Emotions
Female
Humans
Hydrocortisone
Middle Aged
Mindfulness
Motivation
Naltrexone
Narcotic Antagonists
Nausea
Opioid Peptides
Receptors
Opioid
Reward
Stress
Psychological
Weight Reduction Programs
Hedonic eating
Mindfulness intervention
Cortisol
Nutrition & Dietetics
Language
Abstract
There are currently no commonly used or easily accessible 'biomarkers' of hedonic eating. Physiologic responses to acute opioidergic blockade, indexed by cortisol changes and nausea, may represent indirect functional measures of opioid-mediated hedonic eating drive and predict weight loss following a mindfulness-based intervention for stress eating. In the current study, we tested whether cortisol and nausea responses induced by oral ingestion of an opioidergic antagonist (naltrexone) correlated with weight and self-report measures of hedonic eating and predicted changes in these measures following a mindfulness-based weight loss intervention. Obese women (N = 88; age = 46.7 ± 13.2 years; BMI = 35.8 ± 3.8) elected to complete an optional sub-study prior to a 5.5-month weight loss intervention with or without mindfulness training. On two separate days, participants ingested naltrexone and placebo pills, collected saliva samples, and reported nausea levels. Supporting previous findings, naltrexone-induced cortisol increases were associated with greater hedonic eating (greater food addiction symptoms and reward-driven eating) and less mindful eating. Among participants with larger cortisol increases (+1 SD above mean), mindfulness participants (relative to control participants) reported greater reductions in food addiction symptoms, b = -0.95, SE(b) = 0.40, 95% CI [-1.74, -0.15], p = .021. Naltrexone-induced nausea was marginally associated with reward-based eating. Among participants who endorsed naltrexone-induced nausea (n = 38), mindfulness participants (relative to control participants) reported greater reductions in food addiction symptoms, b = -1.00, 95% CI [-1.85, -0.77], p = .024, and trended toward reduced reward-based eating, binge eating, and weight, post-intervention. Single assessments of naltrexone-induced cortisol increases and nausea responses may be useful time- and cost-effective biological markers to identify obese individuals with greater opioid-mediated hedonic eating drive who may benefit from weight loss interventions with adjuvant mindfulness training that targets hedonic eating.